GEMC: Toxicology of Analgesic Agents: Resident Training
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GEMC: Toxicology of Analgesic Agents: Resident Training

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This is a lecture by Dr. Hernan Gomez from the Ghana Emergency Medicine Collaborative. To download the editable version (in PPT), to access additional learning modules, or to learn more about the ...

This is a lecture by Dr. Hernan Gomez from the Ghana Emergency Medicine Collaborative. To download the editable version (in PPT), to access additional learning modules, or to learn more about the project, see http://openmi.ch/em-gemc. Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution Share Alike-3.0 License: http://creativecommons.org/licenses/by-sa/3.0/.

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GEMC: Toxicology of Analgesic Agents: Resident Training GEMC: Toxicology of Analgesic Agents: Resident Training Presentation Transcript

  • Project: Ghana Emergency Medicine Collaborative Document Title: Toxicology of Analgesic Agents Author(s): Hernan Gomez (Hurley Medical Center) License: Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution Share Alike-3.0 License: http://creativecommons.org/licenses/by-sa/3.0/ We have reviewed this material in accordance with U.S. Copyright Law and have tried to maximize your ability to use, share, and adapt it. These lectures have been modified in the process of making a publicly shareable version. The citation key on the following slide provides information about how you may share and adapt this material. Copyright holders of content included in this material should contact open.michigan@umich.edu with any questions, corrections, or clarification regarding the use of content. For more information about how to cite these materials visit http://open.umich.edu/privacy-and-terms-use. Any medical information in this material is intended to inform and educate and is not a tool for self-diagnosis or a replacement for medical evaluation, advice, diagnosis or treatment by a healthcare professional. Please speak to your physician if you have questions about your medical condition. Viewer discretion is advised: Some medical content is graphic and may not be suitable for all viewers. 1
  • Attribution Key for more information see: http://open.umich.edu/wiki/AttributionPolicy Use + Share + Adapt { Content the copyright holder, author, or law permits you to use, share and adapt. } Public Domain – Government: Works that are produced by the U.S. Government. (17 USC § 105) Public Domain – Expired: Works that are no longer protected due to an expired copyright term. Public Domain – Self Dedicated: Works that a copyright holder has dedicated to the public domain. Creative Commons – Zero Waiver Creative Commons – Attribution License Creative Commons – Attribution Share Alike License Creative Commons – Attribution Noncommercial License Creative Commons – Attribution Noncommercial Share Alike License GNU – Free Documentation License Make Your Own Assessment { Content Open.Michigan believes can be used, shared, and adapted because it is ineligible for copyright. } Public Domain – Ineligible: Works that are ineligible for copyright protection in the U.S. (17 USC § 102(b)) *laws in your jurisdiction may differ { Content Open.Michigan has used under a Fair Use determination. } Fair Use: Use of works that is determined to be Fair consistent with the U.S. Copyright Act. (17 USC § 107) *laws in your jurisdiction may differ Our determination DOES NOT mean that all uses of this 3rd-party content are Fair Uses and we DO NOT guarantee that your use of the content is Fair. To use this content you should do your own independent analysis to determine whether or not your use will be Fair. 2
  • Toxicology of: Analgesic Agents 8-24-11 Sarah_Ackerman, flickr 3
  • Core Toxicology Review Acetaminophen Salicylates NSAIDS 4
  • Analgesics   22 y/o male arrives by EMS after found lying next to bed lethargic   Parents note he had taken a benadryl containing med the night before   VS: BP 120/70, RR 28, Temp 100o F, 02 sat 97% on 2L NC   Non focal neuro exam; pt is “agitated, but arousable;” head contusion noted   Labs = pH 7.33, pO2 94, pCO2 25, CPK 19. 4 K, Na 140, K+ 4.1, Cl 107, HCO3 18, SGOT 426, SGPT 100, BUN 18, Cr 2.0, WBC 27 K, ASA 44.6, Acet 10.4, ETOHNeg, UDS Neg, CXR & Head CT nL   Placed on Bicarb drip in ED – and admitted to ICU   Diagnosis = Salicylate toxicity 5
  • Analgesics   Pt arrives to ICU and noted to be increasingly tachypneic and agitated   Multiple doses of ativan and haldol given …   Intubated for respiratory depression   Temps in ICU over next 4 hours = 101.2, 102.3, 105   Decorticate posturing noted   Decision made approx 6 hours after ED presentation to transfer to facility with higher level of care   Ptdeveloped asystole in ambulance   Autopsy findings showed moderate cerebral edema   Postmortem ASA conc = 67 mg/dL, Diphenhydramine = 3.9 mg/dL 6
  • Salicylates Salicylate Bezoar Source undetermined 7
  • Salicylates   18 month old female found playing with an open bottle of “oil of wintergreen”   Parents note child’s shirt has a strong “wintergreen” odor   Upon examination you find a well appearing child with “wintergreen breath” Omer Wazir, flickr 8
  • Salicylates Salicylate Preparations Oil of Wintergreen Methyl Salicylate Salicylate 7000 mg/tsp Bayer Aspirin Acetylsalicylic acid Salicylate 325 mg/tab St. Joseph Children’s Acetylsalicylic acid Salicylate 81 mg/tab Pepto-Bismol Bismuth Subsalicylate Salicylate 131 mg/tsp Excedrin Migraine Acetylsalicylic acid Salicylate 300 mg/tab Source undetermined 9
  • Salicylism Acute   Mild: tinnitus, deafness   Moderate: hyperventilation, N/V, hyperthermia, acidosis, hyper or hypoglycemia   Severe: Severe acidosis, fever, cerebral/ pulmonary edema, renal failure, Sz Chronic   Adult with DJD, child with Kawasaki’s with diarrhea, tinnitus, tachypnea   Higher mortality rates than acute intoxication   Incidence of cerebral and pulmonary edema 10
  • Compartmental Concepts Acute ASA 50 mg/dL with mild symptoms 11
  • Compartmental Concepts Chronic ASA 50 mg/dL, yet very ill 12
  • Salicylates Laboratory Studies (K+), serial salicylate levels until ASA levels fall   Hypoxic? ABG, CXR   MS changes? CT scan   Done nomogram now largely historical   Lytes Source undetermined Done Nomogram 13
  • Salicylates Treatment         Lavage, multi-dose activated charcoal Urinary alkalinization IV hydration, K+ supp Hemodialysis –  –  –  acute > 80-100 mg/dL chronic > 50-60 mg/dL Acidosis, MS changes, cerebral or pulmonary edema, renal failure soccerkrys, flickr 14
  • Whole Bowel Irrigation   Polyethylene glycol   First described in the Pediatric literature*   History of expulsion of button batteries   Very safe track record *Tenenbein M: Source undetermined Whole bowel irrigation for iron poisoning. J Pediatr 1987;111:142-145. 15
  • What is the definition of pKa? The pH of a solution in which the concentrations of ionized and non-ionized drug are equal. HA H+ + A- Cell membranes are more permeable to substances that are in the non-ionized form (lipid soluble) 16
  • Urine Alkalinization Rationale       Some toxins are weak acids –As they pass through glomeruli non ionized forms are reabsorbed back into circulation Alkaline urine causes disassociation of H+ in weak acids Polar forms remain in the renal tubules and are excreted in urine HA H+ + A- Source undetermined 17
  • Acetaminophen Source undetermined 18
  • Acetaminophen   15 yo female with derangement Lt knee while skiing at Vale   She presents to the ED 4 days later with persistent vomiting and myalgias   GI labs were obtained with mildly elevated BUN/CR, SGOT 650, SPGT 525, Total bili = 2.1, direct bili 1.9, BUN 28, Cr 1.5   Dx of viral syndrome with dehydration made   Supportive care with IVF and antiemetics given in ED   Hepatitis panel was drawn and patient was asked to follow up with PMD in 1-2 days   Discharge instructions advised Tylenol as needed for muscle aches and pains 19
  • Acetaminophen   Pt sees PMD 1 day later with no change in symptoms   Returns to the ED with continued emesis, and RUQ pain   Labs = SGOT 8350, SGPT 7960, Total bili = 12.2, PT = 20, Acet conc = 25 µg/mL   NAC started in 2nd ED visit, Pt died within 48 hours Source undetermined   Plaintiff’s attorney wrote: “physician treated the poisoned patient with more poison” 20
  • Acetaminophen Toxicity Result of Metabolism   Sulfation, glucuronidation>>> P-450 system   NAPQI: Product of P-450 is hepatotoxic   NAPQI is detoxified by glutathione, overdose may exceed glutathione stores   Accumulated NAPQI reacts directly with macromolecules causing hepatic cell death 21
  • Acetaminophen Clinical Presentation   Phase I(1/2-24 hrs): Anorexia, nausea, vomiting   Phase II(24-72 hrs): RUQ pain, PT & liver transaminases begin to rise   Phase III(72-96 hrs): Centrilobular necrosis   Phase IV(4d to 2 wks): Complete resolution Source undetermined 22
  • Acetaminophen N-acetylcysteine May act as glutathione substitute   May stimulate glutathione synthesis   May act as free radical scavenger (oxygen-free radicals are liberated by necrotic hepatic tissue)   NAC may optimize tissue oxygen delivery and utilization   HSCH2CHCOOH NHCOCH3 N-acetylcysteine Colin, Wikimedia Commons 23
  • Acetaminophen   4 hrs conc > 150 ug/ml potentially toxic   Toxic levels receive oral NAC 140 mg/kg   Maximal benefit if started within 8-10 hrs   Treatment should not be withheld if delay over 24 hrs! Source undetermined 24
  • Nonsteriodal Anti-inflammatory Drugs Acetic Acids Diclofenac = Voltaren Etodolac = Lodine Indomethacin = Indocin Ketorolac = Toradol Sulindac = Clinoril Tolmetin = Tolectin Fenamates (Anthralic acids) Meclofenamate = Meclomen Mefenamic acid = Ponstel Proprionic Acid Ibuprofen = Motrin Ketoprofen = Actron Naproxen = Naprosyn Oxicams Piroxicam = Feldene Pyrazolones Phenylbutazone = Butazolidine Combination Products Diclofenac/ misoprostol Hydrocodone/ ibuprofen Selective Cox-2 Inhibitors Celecoxib = Celebrex Meloxicam = Mobic Rofecoxib = Vioxx Valdecoxib = Bextra 25
  • NSAIDS         Acetyl salicylic acid developed by Felix Hoffman in 1897 Search for drug with less GI adverse affects led to development of Ibuprofen in 1961 – marketed in US 1974 1984 Ibuprofen available without prescription 1999 First selective Cox-2 inhibitor Rofecoxib introduced; 2004 withdrawn after increased risk for MI and CVAs associated with use 26
  • NSAIDS Pharmacology       Cyclooxygenase (Cox 1& 2) system induces prostaglandins and prostinoids via arachidonic acid Cox 2 induced Prostanoids are part of bodies inflammatory response (cytokines, leukotrienes) Cox 1 produces PGE2 – vasodilator effect in gastric mucosa (promotes perfusion and healing), PGE2 renal sodium regulation and induces renal vasodilation Source undetermined 27
  • NSAIDS Pharmacology       Cox 1: Produces thromboxane (TXA2) – a potent platelet stimulator Cox 2: Produces PGI2 which inhibits platelet function and promotes blood flow Thus inhibiting PGI2, without inhibition of TXA2 may explain increased thrombotic events noted by selective Cox 2 NSAIDS allygirl520, flickr 28
  • NSAIDS Overdose         Cox 2 selective agents (i.e. celecoxib/ celebrex) overdose information is limited Case series of 92 OD patients had drowsiness, agitation, vomiting in only 2% of cases (and no deaths)* Overdose of NSAIDS in general result in no symptoms to altered mental status, seizures Seizure esp common with Mefenamic acid Suggested Reading: Forrester MB. Hum Exp Toxicol 2009; 28: 194-4 29
  • NSAIDS Overdose       Rise in hepatic transaminases and acute renal insufficiency published in case reports – but uncommon Massive acute NSAID OD (usually ibuprofen over 400 mg/kg) may result in death from multisystem organ failure (coma, seizures, hypotension, cardiac dysrthymias) Nomogram proposed historically, but without available labs, and no specific antidote – not used Hall et al. West J Med 1988; 148: 653-656 30
  • NSAIDS Overdose   Emergency Department Care –  Activated charcoal           Consider whole bowel irrigation Monitor vital signs Manage symptoms Since NSAIDS are protein bound there is no role for hemodialysis, hemoperfusion, or hemofiltration *Apply the “Science of supportive care” Suggested Reading: Alvin Bronstein 3rd Edition Medical Toxicology, Chapter 127B, p. 754 31
  • NSAIDS Pitfalls*     Avoid use in pregnancies (esp. 3rd trimester) due to Cox 1 inhibition of PGE2 (potential for premature closure of ductus arteriosis) In OD – most symptoms appear within 4 hours, though few case reports of delayed symptoms Jacob Botter, flickr Suggested Reading: Alvin Bronstein 3rd Edition Medical Toxicology, Chapter 127B 32